Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01480 | A02 | 676925 | G | A | missense_variant | MODERATE | c.1232C>T|p.Ser411Phe |
S43 |
2 | BAA02g01480 | A02 | 677409 | G | A | missense_variant | MODERATE | c.748C>T|p.His250Tyr |
S297 |
3 | BAA02g01480 | A02 | 678305 | C | T | upstream_gene_variant | MODIFIER | c.-149G>A| |
S211 S227 |
4 | BAA02g01480 | A02 | 679431 | G | A | upstream_gene_variant | MODIFIER | c.-1275C>T| |
S260 |
5 | BAA02g01480 | A02 | 679557 | C | T | upstream_gene_variant | MODIFIER | c.-1401G>A| |
S19 |
6 | BAA02g01480 | A02 | 679651 | G | A | upstream_gene_variant | MODIFIER | c.-1495C>T| |
S134 |
7 | BAA02g01480 | A02 | 681754 | G | A | upstream_gene_variant | MODIFIER | c.-3598C>T| |
S23 |